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This paper describes an on-vehicle demonstration of a hydrogen-heated catalyst (HHC) system for reducing the level of cold-start hydrocarbon emissions from a gasoline-fueled light-duty vehicle. The HHC system incorporated an onboard electrolyzer that generates and stores hydrogen (H2) during routine vehicle operation. Stored hydrogen and supplemental air are injected upstream of a platinum-containing automotive catalyst when the engine is started. Rapid heating of the catalytic converter occurs immediately as a result of catalytic oxidation of hydrogen (H2) with oxygen (O2) on the catalyst surface. Federal Test Procedure (FTP) emission results of the hydrogen-heated catalyst-equipped vehicle demonstrated reductions of hydrocarbons (HC) and carbon monoxide (CO) up to 68 and 62 percent, respectively. This study includes a brief analysis of the emissions and fuel economy effects of a 10-minute period of hydrogen generation during the FTP.

An increasing number of passenger vehicle exhaust systems incorporate catalytic converters that are “close-coupled” to the exhaust manifold to further reduce the quantity of cold-start emissions and increase overall catalyst conversion efficiencies. In general, close-coupled catalytic converters are not necessarily subjected to higher inlet exhaust temperatures than conventional underbody catalytic converters. To establish a foundation of on-vehicle temperature data, several passenger vehicles with close-coupled catalytic converters were studied while operating on a chassis dynamometer. Converter temperatures were measured over a variety of vehicle test conditions, including accelerations and extended steady-state speeds for several throttle positions, at both zero- and four-percent simulated road grades.

In order to further reduce vehicle cold-start emissions, the use of catalytic converters that are “close-coupled” to the exhaust manifold is increasing. To understand the vibrational environment of close-coupled and underbody converters, a laboratory study was conducted on several passenger vehicles. Catalytic converter vibration spectra were measured on a chassis dynamometer with the vehicle operating over a variety of test conditions. Vehicle operating conditions included hard accelerations and extended steady-state speeds at distinct throttle positions over zero-percent and four-percent simulated road grades.

Copper ion exchange procedures were used to prepare zeolite-based catalysts for NOx reduction in lean (oxygen-rich) exhaust. Energy dispersive x-ray fluorescence and scanning electron microscopy analyses confirmed the presence of copper in the zeolite matrix. Zeolites were applied onto honeycomb and foam substrates, and evaluated for catalytic NOx reduction efficiency using engine exhaust. Copper-exchanged zeolite catalysts prepared for this study revealed NOx reduction of 95 percent for a period of seven minutes using previously adsorbed exhaust hydrocarbons as the reducing agent. Experiments using ethylene injection to supplement the exhaust suggest long-term and sustained NOx reduction, initially observed at 52 percent. Experimental results and performance comparisons of ZSM-5, mordenite, and Y-type zeolites are discussed. Zeolite catalysts based on Cu-mordenite showed high levels of initial NOx reduction, while results using Cu-ZSM-5 suggested better long-term activity.

This paper describes the findings of a laboratory effort to demonstrate improved automotive exhaust emission control with a cold-start hydrocarbon collection system. The emission control strategy developed in this study incorporated a zeolite molecular sieve in the exhaust system to collect cold-start hydrocarbons for subsequent release to an active catalytic converter. A prototype emission control system was designed and tested on a gasoline-fueled vehicle. Continuous raw exhaust emission measurements upstream and downstream of the zeolite molecular sieve revealed collection, storage, and release of cold-start hydrocarbons. Federal Test Procedure (FTP) emission results show a 35 percent reduction in hydrocarbons emitted during the cold-transient segment (Bag 1) due to adsorption by the zeolite.